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FDA 510(k)

GROUP STREP BROTH T3472 LIM

K-Number: K833759 · 1983-12-16

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1983-12-16
Product CodeJSD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GROUP STREP BROTH T3472 LIM is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1983-12-16 under 510(k) number K833759. The device is classified under product code JSD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GROUP STREP BROTH T3472 LIM?

GROUP STREP BROTH T3472 LIM is a medical device that received FDA 510(k) clearance on 1983-12-16. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K833759.

When did GROUP STREP BROTH T3472 LIM receive FDA 510(k) clearance?

GROUP STREP BROTH T3472 LIM received FDA 510(k) clearance on 1983-12-16, under 510(k) number K833759.

Who is the listed applicant for GROUP STREP BROTH T3472 LIM?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GROUP STREP BROTH T3472 LIM?

The FDA product code for GROUP STREP BROTH T3472 LIM is JSD.

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Related Devices (Code: JSD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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